Data / Medical devices / United States / Exel Inc.
Exel Inc.: FDA-registered device maker in Southaven, MS, United States, 5 510(k) clearances
Exel Inc. is registered with the FDA (registration 3015443199) in Southaven, MS, United States. It lists 12 device types. The FDA files 5 510(k) clearances under its listings, the newest dated April 13, 2017. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3015443199
- Address
- 8655 Commerce Drive Ste 101, Southaven, MS, United States, 38671
- Owner or operator
- Exel Inc. dba DHL Supply Chain (USA) (10026656)
- Roles
- Repackager or relabeler
- First device listed
- April 3, 2019
- Registered through
- 2026
- Brand names listed
- Avanos
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Accessories, Cleaning Brushes, For Endoscope | MNL | 1 | Repackager or relabeler | accessdata.fda.gov |
| Anesthesia Conduction Kit | CAZ | 2 | Repackager or relabeler | accessdata.fda.gov |
| Bag, Drainage, With Adhesive, Ostomy | FON | 1 | Repackager or relabeler | accessdata.fda.gov |
| Catheter, Conduction, Anesthetic | BSO | 2 | Repackager or relabeler | accessdata.fda.gov |
| Catheter, Infusion | JCY | 1 | Repackager or relabeler | accessdata.fda.gov |
| Catheters, Suction, Tracheobronchial | BSY | 1 | Repackager or relabeler | accessdata.fda.gov |
| Endoscope Introducer Kit | NWU | 2 | Repackager or relabeler | accessdata.fda.gov |
| Neurological Tray | OJG | 1 | Repackager or relabeler | accessdata.fda.gov |
| Probe, Radiofrequency Lesion | GXI | 2 | Repackager or relabeler | accessdata.fda.gov |
| Sealant, Microbial | NZP | 2 | Repackager or relabeler | accessdata.fda.gov |
| Tube, Tracheal (W/Wo Connector) | BTR | 2 | Repackager or relabeler | accessdata.fda.gov |
| Tubes, Gastrointestinal (And Accessories) | KNT | 2 | Repackager or relabeler | accessdata.fda.gov |
510(k) clearances
The 510(k) numbers this establishment lists, with the FDA decision on each. The applicant is the company that holds the clearance.
| Decided | 510(k) number | Device | Product code | Decision | Applicant | Source |
|---|---|---|---|---|---|---|
| April 13, 2017 | K163461 | Coolief* Cooled RF Probe | GXI | Substantially Equivalent | Halyard Health, Inc. | accessdata.fda.gov |
| September 30, 2016 | K161232 | ON-Q* EchoSpark Echogenic Catheter; ON-Q* T-bloc* Echogenic Continuous Nerve Block Kit | BSO | Substantially Equivalent | Halyard Health | accessdata.fda.gov |
| August 20, 2013 | K131254 | KIMVENT MICROCUFF SUBGLOTTIC SUCTIONING ENDOTRACHEAL TUBE | BTR | Substantially Equivalent | Kimberly-Clark Corp. | accessdata.fda.gov |
| June 26, 2013 | K122653 | MIC-KEY SF LOW PROFILE GASTROSTOMY TUBE AND ACCESSORIES | KNT | Unknown | Kimberly-Clark Corporation | accessdata.fda.gov |
| September 29, 2006 | K052870 | INTEGUSEAL MICROBIAL SEALANT, MODEL IS 100 AND 1S200 | NZP | Substantially Equivalent | Kimberly-Clark Corp. | accessdata.fda.gov |
Compare with other makers
- All makers of Endoscope Introducer Kit
- All makers of Bag, Drainage, With Adhesive, Ostomy
- All makers of Catheters, Suction, Tracheobronchial
- All makers of Catheter, Infusion
- All makers of Catheter, Conduction, Anesthetic
- All makers of Anesthesia Conduction Kit
Updated April 13, 2017. Read from openFDA bulk downloads (device registration and listing, 510(k), PMA, recall and enforcement files). CC0 1.0, public domain (openFDA terms of service). The files are joined on FDA identifiers: the 510(k) and PMA numbers a registration lists, and the recalling firm's FEI for recalls. Recall class comes from the FDA enforcement report. The FDA states that openFDA data is unvalidated and is not for decisions about medical care. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.